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51083003: Structure showing abnormal deposition of pigment (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
85116019 Pigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85118018 Pigment deposition en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
788943015 Structure showing abnormal deposition of pigment (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2670935014 Structure showing abnormal deposition of pigment en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85116019 Pigmentation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
85116019 Pigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85118018 Pigment deposition en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
85118018 Pigment deposition en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
788943015 Structure showing abnormal deposition of pigment (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
788943015 Structure showing abnormal deposition of pigment (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2670935014 Structure showing abnormal deposition of pigment en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2670935014 Structure showing abnormal deposition of pigment en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


36 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure showing abnormal deposition of pigment (morphologic abnormality) Is a Deposition true Inferred relationship Existential restriction modifier (core metadata concept)
Structure showing abnormal deposition of pigment (morphologic abnormality) Is a Pigment alteration true Inferred relationship Existential restriction modifier (core metadata concept)
Structure showing abnormal deposition of pigment (morphologic abnormality) Is a Lesion of degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Diffuse tenosynovial giant cell tumor of first metatarsophalangeal joint Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Diffuse tenosynovial giant cell tumour of talonavicular joint Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Villonodular synovitis of ankle Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented oral mucosal lesion Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Iron pigmentation of oral mucosa Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Exogenous pigmentation of oral mucosa Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Systemic exogenous pigmentation of oral mucosa Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Local exogenous pigmentation of oral mucosa Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Laugier-Hunziker syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrial myxoma with lentigines Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Genital lentiginosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple lentigines syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Pigmentation of oral mucosa (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentigo maligna Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Exogenous ochronosis (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ochronotic arthritis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular albinism-lentigines-deafness syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Peutz-Jeghers polyps of small bowel Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 4
Peutz-Jeghers syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 4
lentigo Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Lentiginosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital/hereditary lentiginosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Buccal pigmentation due to Addison's disease (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ochronosis caused by hydroquinone (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Nevoid lentiginosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Zosteriform lentiginosis (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Drug-induced oral pigmentation (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Villonodular synovitis of hip Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Villonodular synovitis of hip Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Villonodular synovitis of knee Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Villonodular synovitis of knee Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Villonodular synovitis of ankle Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Villonodular synovitis of ankle Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse tenosynovial giant cell tumour of talonavicular joint Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse tenosynovial giant cell tumour of talonavicular joint Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse tenosynovial giant cell tumor of first metatarsophalangeal joint Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Diffuse tenosynovial giant cell tumor of first metatarsophalangeal joint Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented xerodermoid Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented xerodermoid Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Pigmented scar Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Mercury pigmentation of skin Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Carotene pigmentation of skin (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chrysoderma (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival adrenochrome deposits (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Corneal pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmentation of oral mucosa (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival argyrosis Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group F Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented oral mucosal lesion Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Exogenous pigmentation of oral mucosa Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Local exogenous pigmentation of oral mucosa Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group A Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Carotene pigmentation of skin (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival pigmentation (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chlorpromazine pigmentation Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired anterior capsular pigmentation (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Mercury pigmentation of skin Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented xerodermoid Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group G Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Stromal corneal pigmentation Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chrysoderma (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Anterior corneal pigmentation Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group D Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group B Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Drug-induced oral pigmentation (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Progressive pigmentary dermatosis of Schamberg Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Buccal pigmentation due to Addison's disease (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival adrenochrome deposits (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ochronotic arthritis Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Laugier-Hunziker syndrome Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Corneal pigmentation Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-neurologic xeroderma pigmentosum Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group C (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group E (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, variant form Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Iron pigmentation of oral mucosa Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Systemic exogenous pigmentation of oral mucosa Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Meconium pigmentation (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 4
Amalgam tattoo Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Local exogenous pigmentation of oral soft tissue Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chlorpromazine pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Drug-induced oral pigmentation (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Conjunctival adrenochrome deposits (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
ictère périnatal causé par une hémolyse excessive Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group B Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Non-neurologic xeroderma pigmentosum Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Pigmented xerodermoid Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, group C (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, group G Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, group F Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, group A Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, group E (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, group D Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum, variant form Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome. Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 5
Pigment dispersion syndrome of bilateral eyes (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Pigment dispersion syndrome of bilateral eyes (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3

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